Granted Patent B2

US 7,482,113 · App. 11/611,914 · Granted Jan 27, 2009

Abstract

Claims (58)

1. A photothermographic material comprising a support having on at least one side thereof, one or more photothermographic imaging layers comprising in reactive association:

a. a photosensitive silver halide,

b. a non-photosensitive source of reducible silver ions,

c. a reducing agent composition for said reducible silver ions comprising a trisphenol reducing agent represented by the following Structure (I),

d. a polymeric binder, and

e. a substituted olefinic co-developer that is represented by the following Structure (IV):

wherein L 1 and L 2 are independently sulfur or a mono-substituted or unsubstituted methylene group,

R 1 and R 2 are independently primary or secondary substituted or unsubstituted alkyl groups having 1 to 12 carbon atoms,

R 3 , R 4 , and R 5 are independently substituted or unsubstituted alkyl groups having 1 to 12 carbon atoms, substituted or unsubstituted alkoxy groups having 1 to 12 carbon atoms, or halo groups, and

R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 are independently hydrogen or any substituent that is substitutable on a benzene ring,

wherein V and W are independently aromatic or electron withdrawing groups, provided that at least one of V and W is an electron withdrawing group, or V and W can represent the atoms necessary to form a ring containing an electron withdrawing group,

R is an —O − A + or —S − A + group, and

A + is a quaternary phosphonium cation.

2. The photothermographic material of claim 1 wherein L 1 and L 2 are independently a methylene group or a mono-substituted methylene group, R 1 and R 2 are independently substituted or unsubstituted primary or secondary alkyl groups having 1 to 8 carbon atoms, R 3 , R 4 , and R 5 are independently substituted or unsubstituted alkyl groups having 1 to 6 carbon atoms, and R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 are independently hydrogen, or substituted or unsubstituted methyl, ethyl, or methoxy groups, or chloro groups.

3. The photothermographic material of claim 1 wherein L 1 and L 2 are unsubstituted methylene groups, R 1 and R 2 are the same substituted or unsubstituted primary or secondary alkyl groups, R 3 , R 4 , and R 5 are the same substituted or unsubstituted methyl or ethyl groups, and R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 are independently hydrogen or unsubstituted methyl groups.

4. The photothermographic material of claim 1 wherein said reducing agent of Structure (I) is present in an amount of at least 0.5 mmol/m 2 .

5. The photothermographic material of claim 1 wherein said substituted olefinic co-developer is present at a molar ratio to said reducing agent of Structure (I) of from about 0.001:1 to about 0.02:1.

6. The photothermographic material of claim 1 wherein V is a carboalkoxy group having 2 to 20 carbon atoms, a carboxamido group having 2 to 20 carbon atoms, or a carbocyclic or heterocyclic aryl group having 6 to 10 atoms in the ring, W is a cyano group, and R is an —O − A + group.

7. The photothermographic material of claim 1 wherein said quaternary phosphonium cation A + is represented by either of the following Structures (V) and (VI):

wherein R 25 through R 28 are independently alkyl or aryl groups, and R 29 is an alkylene or arylene group.

8. The photothermographic material of claim 7 wherein R 25 through R 28 are each the same or different phenyl groups, or at least one of R 25 through R 28 is a benzyl group and the rest are the same or different phenyl groups, R 29 is an alkylene group having 1 to 10 carbon atoms in the chain or a 1,2-, 1,3-, or 1,4-substituted phenyl group.

9. The photothermographic material of claim 1 wherein V is a carboalkoxy group having 2 to 9 carbon atoms, a carboxamido group having 2 to 7 carbon atoms, or a halogen-substituted phenyl group, and A + is a tetraphenylphosphonium or benzyltriphenylphosphonium ion.

10. The photothermographic material of claim 1 comprising one or more of the following substituted olefinic co-developers CDP-1, CDP-3, CDP-4, CDP-5, CDP-11, and CDP-12:

11. The photothermographic material of claim 1 wherein the total amount of silver is from about 1 to about 2.6 g/m 2 .

12. The photothermographic material of claim 1 further comprising at least one additional reducing agent that is a monophenol or a bisphenol, or both.

13. The photothermographic material of claim 1 further comprising a protective overcoat layer disposed over said photothermographic layer, and interlayer, carrier layer, or any combination thereof.

14. The photothermographic material of claim 1 that provides a silver black-and-white image.

15. The photothermographic material of claim 1 wherein said photothermographic imaging layer has been coated out of an organic solvent and said polymeric binder is a hydrophobic binder that is soluble in said organic solvent.

16. The photothermographic material of claim 1 wherein said photosensitive silver halide is silver bromide or a silver iodobromide that is present predominantly in cubic or tabular grains,

said non-photosensitive source of reducible silver ions comprises at least silver behenate,

said polymeric binder is a polyvinyl butyral or polyvinyl acetal binder, and

said substituted olefinic co-developer is one or more of CDP-1, CDP-3, CDP-4, CDP-5, CDP-11, and CDP-12 shown below,

said trisphenol reducing agent is Compound I-2 or I-3 as represented by Structure I in which R 1 -R 5 , L 1 , and L 2 are as shown below and is present in an amount of from about 1 to about 5 mmol/m 2 ,

said substituted olefinic co-developer is present in an amount of from about 0.005 to about 0.02 mmol/m 2 , and the molar ratio of said substituted olefinic co-developer to said trisphenol reducing agent is from about 0.001:1 to about 0.02:1, and

the total amount of silver is present in an amount of at least 1 g/m 2 and less than or equal to 2.6 g/m 2 ,

Trisphenol

Reducing

Agent

R 1 , R 2

R 3 , R 5

R 4

L 1 , L 2

I-2

CH 3

CH 3

CH 3

CH 2

I-3

Cyclohexyl

CH 3

CH 3

CH 2 .

17. The photothermographic material of claim 16 further comprising at least one additional reducing agent that is a bisphenol.

18. A method of forming a visible image comprising:

A) imagewise exposing the photothermographic material of claim 1 to electromagnetic radiation to form a latent image, and

B) simultaneously or sequentially, heating said exposed photothermographic material to develop said latent image into a visible image.

19. The method of claim 18 wherein said imagewise exposing is carried out using laser imaging at from about 600 to about 1200 nm or said development is carried out for at least 3 and up to and including 25 seconds, to provide a visible black-and-white image.

20. The method of claim 18 wherein said photothermographic material comprises one or more of the following substituted olefinic co-developers CDP-1, CDP-3, CDP-4, CDP-5, CDP-11, and CDP-12:

Assignments (9)